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Impact of Perioperative Intravenous Fluid Utilization on Postoperative Outcomes

NCT01563991 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 186

Last updated 2017-03-30

No results posted yet for this study

Summary

Subjects undergoing surgery on the small or large bowel will be randomized to one of 2 groups, a normal fluid amount group and a reduced fluid amount group to evaluate the impact of this change on recovery after surgery.

Conditions

  • Benign Neoplasm of Intestinal Tract
  • Primary Malignant Neoplasm of Intestinal Tract
  • Secondary Malignant Neoplasm of Intestinal Tract

Interventions

PROCEDURE

Normal fluid volume

Normal fluid group will receive lactated ringes at 8 cc / Kg/ hr total

PROCEDURE

Reduced fluid volume

Subject receives 80 cc/ hr LR during the peri-operative period

Sponsors & Collaborators

  • The Cleveland Clinic

    lead OTHER

Principal Investigators

  • Lucci Stocchi, MD · The Cleveland Clinic

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-02-28
Primary Completion
2012-04-18
Completion
2012-04-18

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01563991 on ClinicalTrials.gov